HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659215A>T , CM000685.2:g.136659215A>T | GRCh38 |
NC_000023.10:g.135741374A>T , CM000685.1:g.135741374A>T | GRCh37 |
NC_000023.9:g.135569040A>T | NCBI36 |
NG_007280.1:g.16039A>T , LRG_141:g.16039A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*204A>T | ENSP00000512122.1:n.*204A>T | |
ENST00000695725.1:c.*141A>T | ENSP00000512123.1:n.*141A>T | |
ENST00000695726.1:n.2554A>T | ||
ENST00000695729.1:n.3389A>T | ||
ENST00000370629.7:c.586A>T MANE Select | ENSP00000359663.2:p.Lys196Ter | |
ENST00000370628.2:c.523A>T | ENSP00000359662.2:p.Lys175Ter | |
ENST00000370629.6:c.586A>T | ENSP00000359663.2:p.Lys196Ter | |
NM_000074.2:c.586A>T , LRG_141t1:c.586A>T | NP_000065.1:p.Lys196Ter | |
NM_000074.3:c.586A>T MANE Select | NP_000065.1:p.Lys196Ter |